Adult Tic Disorders Registry

Assistance Publique - Hôpitaux de Paris450 enrolled

Overview

The purpose of this study is to develop the adult tic disorders registry in order to characterize the relationship between tic severity and tic-related impairment in women compared to men with tic disorders.

Study Type

OBSERVATIONAL

Enrollment

450

Conditions

Tic Disorders

Interventions

QOL to be completed by the participantOTHER

The scales (PUTS, OCI, TS-QOL, ASRS, GAD-7, PHQ9, TAPS) to be completed by the participant

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion criteria : 1. Age \>18 years 2. Patients with Tic disorders 3. Given the non-opposition Non Inclusion criteria 1. No affiliation to a French health social insurance 2. Significant congenital disorders that may affect understanding of assessments 3. Patients under guardianship or curatorship

Locations (7)

CHU Clermont-Ferrand

Clermont-Ferrand, France

RECRUITING

CHU Limoges

Limoges, France

RECRUITING

CHU Marseille

Marseille, France

Outcomes

Primary Outcomes

Correlation between Quality of Life and TICs severity

Severity of the tics measurement (YGTSS Impairment Score) and the quality of life (TS-QOL) between men and women with tic disorders, while controlling for the YGTSS Total Tic Score

Time frame: 6 months

Secondary Outcomes

Change in TICs

Change in tic inventories/tic migrations with the YGTSS tic inventories

Time frame: 6 months

Central Contacts

Emmanuel Flamand-Roze, MD, PhD

CONTACT

1 42 16 06 45 emmanuel.flamand-roze@aphp.fr

Data from ClinicalTrials.gov

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